Clinical Research Associate

Kelly Science, Engineering, Technology & Telecom; São Paulo; Presencial; BRL 120 000 - 180 000; Tempo integral

Resumo da oferta

Kelly Science, Engineering, Technology & Telecom in Brazil is actively sourcing for a Clinical Research Associate (CRA) to join a pipeline opportunity with a global life sciences leader. The role focuses on overseeing clinical trials across sites, ensuring protocol and GCP compliance, and maintaining high data quality.

Ideal candidates have a life sciences degree and 3–7 years’ CRA experience, with strong attention to detail, communication skills, and willingness to travel.

Qualificações

• Bachelor’s degree in life sciences or related field is required.
• 3–7 years’ experience as a CRA or in clinical research.
• Solid knowledge of GCP and regulatory guidelines.
• Excellent attention to detail and strong organizational skills.
• Willingness to travel frequently.

Responsabilidades

• Conduct site visits to ensure protocol adherence and regulatory compliance.
• Verify data and documentation are accurate and maintained per GCP.
• Identify and resolve site issues related to safety or protocol.
• Serve as liaison between sponsor and investigative sites.
• Review Trial Master File documents and maintain monitoring reports.
• Train site staff on study procedures and requirements.
• Ensure timely reporting of adverse events and deviations.
• Assist in subject recruitment and retention strategies.
• Communicate findings to stakeholders.

Conhecimentos

CRA experience

GCP knowledge

Clinical research

Formação académica

Bachelor's degree in life sciences

Ferramentas

EDC platforms

Descrição da oferta de emprego

Job Title: Clinical Research Associate (CRA)

Start: To be Confirmed (Pipeline Opportunity)

Organisation: Leading global life sciences company (via Kelly FSP)

Job Overview:

Kelly is pipelining talent for an evergreen CRA role in pharma. If you’re looking for a project-based career as a CRA, we’d love to have a preliminary conversation, connect with us to explore future opportunities!

This is a pipeline opportunity for proactive candidates interested in joining a global leader in the life sciences industry.

The Clinical Research Associate (CRA) is responsible for overseeing clinical trials and ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. The CRA monitors the progress of clinical studies conducted at investigative sites and ensures that data is collected, recorded, and reported accurately.

Key Responsibilities:

• Conduct site visits (initiation, monitoring, and closeout) to ensure adherence to study protocols and regulatory requirements.
• Verify that study data and documentation are accurate, complete, and maintained according to GCP.
• Identify, resolve, and elevate site issues related to protocol compliance or subject safety.
• Act as the primary liaison between the sponsor and investigative sites.
• Review and collect essential documents for the Trial Master File.
• Train and support site staff on study procedures and protocol requirements.
• Ensure timely reporting of adverse events and deviations.
• Assist in subject recruitment and retention strategies.
• Prepare and maintain accurate monitoring reports and documentation.
• Communicate findings and follow-up activities to stakeholders.

Qualifications:

• Bachelor’s degree in life sciences, pharmacy, or relevant field (required).
• Prior experience as a CRA or in clinical research (3-7 years)
• Knowledge of Good Clinical Practice (GCP) and relevant regulatory guidelines.
• Strong attention to detail and organizational skills.
• Effective written and verbal communication abilities.
• Ability to travel frequently.

Preferred Skills:

• Familiarity with Electronic Data Capture (EDC) platforms.
• Problem-solving and conflict resolution.
• Ability to work independently and in a team environment.
• 3-7 years as a CRA

Why Join?

• Opportunity to join a globally recognised life sciences company through Kelly’s FSP model.
• Work with international experts on high-impact projects.
• Gain global exposure and expand your clinical knowledge.
• Be part of a collaborative, growth-focused work culture.
• Pipeline opportunity with anticipated hiring in the near future, apply early to be considered once the position is formally approved and released.